20-25 Year Follow-Up on Regenerative Bone Procedures for Peri-Implantitis

Sponsor
Kristianstad University
Study ID
NCT06648564
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Interventions

  • Bone regenerative surgery with a bone graft substitute and a resorbable membrane — PROCEDURE
    Dental implants with a diagnosis peri-implantitis were treated with regenerative surgery.

Study Details

The goal of this 20-25-year observational study is to investigate the outcomes of bone regenerative surgery in peri-implantitis. Two different techniques will be compared: surgery with a bone substitute alone and surgery with a bone substitute combined with a membrane, to determine their effectiveness and assess whether one is more effective than the other. The intention of this observational study is to learn more about the long-term effects of bone regenerative surgery in patients with peri-implantitis. Patients will be called in for a clinical and radiographic examination of the surgically treated implant(s). Probing pocket depths, presence of pus, bleeding around the implant (s) and a radiograph of the implant (s). To be able to compare with the 1, 3, 5 and 10 year measurements.

Key Dates

Start date
Aug 31, 2025
Status verified
Feb 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025

Study Design

Enrollment
20 participants (estimated)

Arms

  • Arm: Group 1
    Bone regenerativ surgery with a bone graft material (Algipore) and a resorbable membrane (Osseoquest)
  • Arm: Group 2
    Bone regenerativ surgery with a bone graft material (Algipore)

Primary Outcome Measure

Bone fill [ Time Frame: Ten years after surgical regenerative boneprocedures ]

Related Studies